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What is Chromosome 9 inversion or duplication?

What is Chromosome 9 inversion or duplication?

  • Chromosome 9 inversion or duplication: A very rare genetic disorder where a portion of chromosome 9 is inverted or duplicated which results in various abnormalities. The type and severity of symptoms varies depending on the size and location of the genetic material involved.

Chromosome 9 inversion or duplication is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 9 inversion or duplication, or a subtype of Chromosome 9 inversion or duplication, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Chromosome 9 inversion or duplication: Introduction

Types of Chromosome 9 inversion or duplication:

Broader types of Chromosome 9 inversion or duplication:

How serious is Chromosome 9 inversion or duplication?

Prognosis of Chromosome 9 inversion or duplication: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.

What causes Chromosome 9 inversion or duplication?

Causes of Chromosome 9 inversion or duplication: see causes of Chromosome 9 inversion or duplication

What are the symptoms of Chromosome 9 inversion or duplication?

Symptoms of Chromosome 9 inversion or duplication: see symptoms of Chromosome 9 inversion or duplication

How is it treated?

Doctors and Medical Specialists for Chromosome 9 inversion or duplication: Medical Geneticist ; see also doctors and medical specialists for Chromosome 9 inversion or duplication.
Treatments for Chromosome 9 inversion or duplication: see treatments for Chromosome 9 inversion or duplication

Name and Aliases of Chromosome 9 inversion or duplication

Main name of condition: Chromosome 9 inversion or duplication

Other names or spellings for Chromosome 9 inversion or duplication:

Trisomy 9 translocation

Trisomy 9 translocation
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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